Description
The Clinical Project Manager will plan, organize, and oversee clinical trials from an international Clinical Operations team, coordinating cross-functional internal teams and third-party vendors, managing budgets and project plans, leading study teams, communicating with sponsors, addressing quality issues through corrective and preventive actions, and supporting proposals and bid defenses. The role requires approximately five years of clinical research experience, project and study team management expertise, fluent English, and familiarity with clinical technology systems such as CTMS, EDC, IXRS, eTMF, and project planning tools; early-phase and oncology experience is advantageous. The position is available in any European Union country and offers remote work, flexibility, bonuses, wellness initiatives, professional development, and insurance benefits.
